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Fusion gene ID: 35771 |
FusionGeneSummary for SPP1_THSD4 |
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Fusion gene information | Fusion gene name: SPP1_THSD4 | Fusion gene ID: 35771 | Hgene | Tgene | Gene symbol | SPP1 | THSD4 | Gene ID | 30827 | 79875 |
Gene name | CXXC finger protein 1 | thrombospondin type 1 domain containing 4 | |
Synonyms | 2410002I16Rik|5830420C16Rik|CFP1|CGBP|HsT2645|PCCX1|PHF18|SPP1|ZCGPC1|hCGBP | ADAMTSL-6|ADAMTSL6|FVSY9334|PRO34005 | |
Cytomap | 18q21.1 | 15q23 | |
Type of gene | protein-coding | protein-coding | |
Description | CXXC-type zinc finger protein 1CXXC finger 1 (PHD domain)CpG binding proteinDNA-binding protein with PHD finger and CXXC domainPHD finger and CXXC domain-containing protein 1cpG-binding proteinzinc finger, CpG binding-type containing 1 | thrombospondin type-1 domain-containing protein 4A disintegrin and metalloproteinase with thrombospondin motifs-like protein 6ADAMTS-like protein 6thrombospondin, type I, domain containing 4 | |
Modification date | 20180523 | 20180519 | |
UniProtAcc | P10451 | Q6ZMP0 | |
Ensembl transtripts involved in fusion gene | ENST00000237623, ENST00000395080, ENST00000360804, ENST00000509659, | ENST00000355327, ENST00000261862, ENST00000357769, ENST00000567838, | |
Fusion gene scores | * DoF score | 6 X 4 X 5=120 | 22 X 7 X 13=2002 |
# samples | 6 | 22 | |
** MAII score | log2(6/120*10)=-1 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(22/2002*10)=-3.18586654531133 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: SPP1 [Title/Abstract] AND THSD4 [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | SPP1 | GO:0006355 | regulation of transcription, DNA-templated | 10688657 |
Hgene | SPP1 | GO:0045893 | positive regulation of transcription, DNA-templated | 10688657 |
Hgene | SPP1 | GO:0051568 | histone H3-K4 methylation | 17355966 |
![]() (ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018)) * All genome coordinats were lifted-over on hg19. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
Data type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
TCGA | RV | LUSC | TCGA-92-8063-01A | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
5CDS-3UTR | ENST00000237623 | ENST00000355327 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
5CDS-3UTR | ENST00000237623 | ENST00000261862 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
5CDS-intron | ENST00000237623 | ENST00000357769 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
5CDS-intron | ENST00000237623 | ENST00000567838 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
intron-3UTR | ENST00000395080 | ENST00000355327 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
intron-3UTR | ENST00000395080 | ENST00000261862 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
intron-intron | ENST00000395080 | ENST00000357769 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
intron-intron | ENST00000395080 | ENST00000567838 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
intron-3UTR | ENST00000360804 | ENST00000355327 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
intron-3UTR | ENST00000360804 | ENST00000261862 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
intron-intron | ENST00000360804 | ENST00000357769 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
intron-intron | ENST00000360804 | ENST00000567838 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
intron-3UTR | ENST00000509659 | ENST00000355327 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
intron-3UTR | ENST00000509659 | ENST00000261862 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
intron-intron | ENST00000509659 | ENST00000357769 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
intron-intron | ENST00000509659 | ENST00000567838 | SPP1 | chr4 | 88904562 | + | THSD4 | chr15 | 72072881 | + |
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FusionProtFeatures for SPP1_THSD4 |
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Hgene | Tgene |
SPP1 | THSD4 |
Promotes FBN1 matrix assembly. Attenuates TGFBsignaling, possibly by accelerating the sequestration of largelatent complexes of TGFB or active TGFB by FBN1 microfibrilassembly, thereby negatively regulating the expression of TGFBregulatory targets, such as POSTN (By similarity). {ECO:0000250}. |
![]() * Minus value of BPloci means that the break pointn is located before the CDS. |
- In-frame and retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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FusionGeneSequence for SPP1_THSD4 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
* Fusion transcript sequences (only coding sequence (CDS) region). |
* Fusion transcript sequences (Full-length transcript). |
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FusionGenePPI for SPP1_THSD4 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
SPP1 | SGTA, PDLIM7, CTNNBL1, IGFBP5, UBQLN4, BAG6, RBBP6, EIF3K, C1RL, COMMD1, COPS5, NCSTN, USP42, CISD2, USP8, AFF4, AMOTL2, DCX, EEF1A1, CEP162, MAP1A, MAP1B, MARCKS, NCKAP1, RANBP9, SEC24C, STAU1, TUBB, DNAJB1, TTC1, PRKACB, STK39, GRIPAP1, RAPGEF2, TPT1, TBC1D8, CC2D1B, CMTM3, MRPL23, RPL5, RPL13, RPL15, RPS13, RIMS4, SNAPIN, ATP2A2, CACNG4, CALM1, LRRC4, ATP5F1, CHD1, DNTTIP2, EPAS1, HMGN1, SLC39A6, ZNF638, BRD3, C2orf50, CYB5R3, DSEL, FTH1, HBA2, KCNIP1, MPPED1, PEMT, PLD3, NACA, SSB, TMEM168, TMEM30A, ZNF804A, APOA1, PEPD, PARP1, MEOX2, ITGAV, ITGB1, ITGB5, F2, TRAF3, RSC1A1 | THSD4 | ZNF195, ALMS1, KRBA1, CEP164, GLI3, ZNF609, FOXG1, APPBP2, HSPA8, USP54, OFD1, RIPK1, ARID5B, MLF1, NUFIP2, HELZ, KANK2, VSIG8, HSPA2 |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for SPP1_THSD4 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for SPP1_THSD4 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | SPP1 | C0001418 | Adenocarcinoma | 2 | CTD_human |
Hgene | SPP1 | C0003949 | Asbestosis | 2 | CTD_human |
Hgene | SPP1 | C0006663 | Calcinosis | 2 | CTD_human |
Hgene | SPP1 | C0022650 | Kidney Calculi | 2 | CTD_human |
Hgene | SPP1 | C0024121 | Lung Neoplasms | 2 | CTD_human |
Hgene | SPP1 | C0025500 | Mesothelioma | 2 | CTD_human |
Hgene | SPP1 | C1458155 | Mammary Neoplasms | 2 | CTD_human |
Hgene | SPP1 | C2609414 | Acute kidney injury | 2 | CTD_human |
Hgene | SPP1 | C0006118 | Brain Neoplasms | 1 | CTD_human |
Hgene | SPP1 | C0017638 | Glioma | 1 | CTD_human |
Hgene | SPP1 | C0017668 | Focal glomerulosclerosis | 1 | CTD_human |
Hgene | SPP1 | C0018799 | Heart Diseases | 1 | CTD_human |
Hgene | SPP1 | C0018824 | Heart valve disease | 1 | CTD_human |
Hgene | SPP1 | C0020517 | Hypersensitivity | 1 | CTD_human |
Hgene | SPP1 | C0022658 | Kidney Diseases | 1 | CTD_human |
Hgene | SPP1 | C0023890 | Liver Cirrhosis | 1 | CTD_human |
Hgene | SPP1 | C0023896 | Alcoholic Liver Diseases | 1 | CTD_human |
Hgene | SPP1 | C0023904 | Liver Neoplasms, Experimental | 1 | CTD_human |
Hgene | SPP1 | C0024668 | Mammary Neoplasms, Experimental | 1 | CTD_human |
Hgene | SPP1 | C0027627 | Neoplasm Metastasis | 1 | CTD_human |
Hgene | SPP1 | C0027659 | Neoplasms, Experimental | 1 | CTD_human |
Hgene | SPP1 | C0030286 | Pancreatic Diseases | 1 | CTD_human |
Hgene | SPP1 | C0032229 | Pleural Neoplasms | 1 | CTD_human |
Hgene | SPP1 | C0032285 | Pneumonia | 1 | CTD_human |
Hgene | SPP1 | C0033687 | Proteinuria | 1 | CTD_human |
Hgene | SPP1 | C0034069 | Pulmonary Fibrosis | 1 | CTD_human |
Hgene | SPP1 | C0041755 | Adverse reaction to drug | 1 | CTD_human |
Hgene | SPP1 | C0041948 | Uremia | 1 | CTD_human |
Hgene | SPP1 | C0162820 | Dermatitis, Allergic Contact | 1 | CTD_human |
Hgene | SPP1 | C0221204 | Lytic lesion | 1 | CTD_human |
Hgene | SPP1 | C0270612 | Leukoencephalopathies | 1 | CTD_human |
Hgene | SPP1 | C0853897 | Diabetic Cardiomyopathies | 1 | CTD_human |
Hgene | SPP1 | C2937358 | Cerebral Hemorrhage | 1 | CTD_human |
Hgene | SPP1 | C4277682 | Chemical and Drug Induced Liver Injury | 1 | CTD_human |
Tgene | THSD4 | C0236969 | Substance-Related Disorders | 1 | CTD_human |